| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148152-45148476 | Common:1; Rare:92 | ||||
| chr17:45490716-45490880 | Rare:55 | ||||
| chr17:47189242-47189494 | Rare:65 | ||||
| chr17:47941356-47941712 | Rare:97; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048045-48048394 | Common:1; Rare:94 | ||||
| chr17:49788640-49788759 | Common:1; Rare:45 | ||||
| chr17:50186315-50186923 | Common:2; Rare:169; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188536-50189017 | Rare:122; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189169-50189448 | Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:50192646-50192807 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192825-50193039 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194829 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195266-50195667 | Rare:109; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50196161-50196318 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50198181-50198504 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |